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5343-16-8

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5343-16-8 Usage

Chemical structure

A derivative of tetrahydrofuran, a cyclic ether, with an amine and methyl group attached.

Functional groups

Contains a tetrahydrofuran ring, amine group (-NH2), and a methyl group (-CH3).

Molecular weight

Approximately 159.23 g/mol

Appearance

Likely a colorless to pale-colored liquid or solid, depending on the conditions.

Solubility

Soluble in organic solvents such as ethanol, methanol, and dichloromethane.

Stability

Stable under normal temperature and pressure conditions, but may decompose upon exposure to heat, light, or strong acids and bases.

Reactivity

Can undergo various chemical reactions, such as nucleophilic substitution, electrophilic addition, and amide bond formation.

Organic synthesis

Used as a building block or reagent in the synthesis of more complex organic molecules.

Pharmaceutical research

Potentially used in the development of new drugs and pharmaceutical compounds.

Industrial purposes

Utilized in the synthesis of various organic molecules for different industries.

Safety precautions

Handle with care, as it may have potential hazards depending on its concentration, exposure, and specific application. Use appropriate personal protective equipment (PPE) and follow safety guidelines when working with this compound.

Storage

Store in a cool, dry, and well-ventilated area, away from heat, light, and strong acids or bases.

Regulatory status

Its regulatory status may vary depending on the country and specific application, so it is essential to consult local regulations and guidelines for proper handling and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 5343-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5343-16:
(6*5)+(5*3)+(4*4)+(3*3)+(2*1)+(1*6)=78
78 % 10 = 8
So 5343-16-8 is a valid CAS Registry Number.

5343-16-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tetrahydro-N-[(tetrahydro-2-furanyl)methyl]-2-furanmethanamine

1.2 Other means of identification

Product number -
Other names bis-tert-butyl biphenylphosphine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5343-16-8 SDS

5343-16-8Downstream Products

5343-16-8Relevant articles and documents

MANUFACTURING METHOD OF AROMATIC COMPOUND AND FURAN DERIVATIVE HAVING METHYLAMINO GROUP

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Paragraph 0028, (2017/10/26)

PROBLEM TO BE SOLVED: To provide a method for manufacturing an aromatic compound or a furan derivative where only aldehyde group is converted to an aminomethyl group while maintaining a structure of aromatic or furan ring from an aromatic compound or a furan derivative having an aldehyde group, capable of being conducted in a water solvent containing no organic solvent and relatively low in by-product. SOLUTION: Amine or ammonia is added in water at first to convert to imine, then a reaction is conducted by using compressive hydrogen with a pressure of 0.1 MPa to 4 MPa in the presence of a metal carried solid catalyst carrying one or more kind of metal selected from rhodium, palladium and platinum or an alloy containing these metal elements. SELECTED DRAWING: Figure 2 COPYRIGHT: (C)2017,JPOandINPIT

Reaction of tetrahydrofurfuryl alcohol with ammonia and hydrogen on heterogeneous catalysts

Glebov,Kliger,Shuikin,Zaikin

, p. 346 - 352 (2007/10/03)

A study has been made of the vapour-phase reaction of tetrahydrofurfuryl alcohol with ammonia and hydrogen on Cu-, Ni-, Co- and Fe-containing bifunctional catalysts at a temperature of 180-240°C. It has been established that, irrespective of the type of catalyst, the main reaction products are piperidine, tetrahydrofurfurylamine and their derivatives. Copyright

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